Lithium Carbonate
- Product NDC
- 0143-1300
- 11-digit product format
- 001431300
- Labeler code
- 0143
- Product ID
- 0143-1300_f27a8c61-3d94-4e67-ade6-7602badc6e0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lithium Carbonate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- West-Ward Pharmaceutical Corp
- Application
- ANDA078715
- Marketing category
- ANDA
- Marketing start
- 2010-12-28
- Marketing end
- 0000-00-00
- Substance
- LITHIUM CARBONATE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record